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The Four Words That Changed My Life

Morgan Greene shares her MG journey, starting with the memorable moment her diagnosis was confirmed.*

One relentless illness. Three unstoppable people.

A Mystery to Me

A Myasthenia Gravis Docuseries

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Join MGFA TOGETHER WE STAND virtual event on Saturday, October 10, 2020. LEARN MORE

OUR MISSION

MG RAISES QUESTIONS.
LOTS OF THEM.

MG United began as a conversation with people in the MG community. This is what we heard. And it’s why we’re here.

If you have MG, you have a story to tell.

Every person living with MG has a story that may help others in similar situations. We’d like to hear yours.

SEE HOW MG RESEARCH IS PUSHING FORWARD. (WE HAVE AN APP FOR THAT.)

MyRealWorld™ MG allows patients to contribute to research firsthand by recording and directly sharing their MG symptoms and treatments with researchers.

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*Paid contributor to MG United

MG United provides news and information for people with myasthenia gravis and the people who love them. But it does not provide medical advice. Always go to your physician, neurologist or other appropriate health professional for individual guidance, diagnosis and treatment.

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